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1.
  • Hagforsen, Eva, et al. (author)
  • Palmoplantar pustulosis : an autoimmune disease precipitated by smoking
  • 2002
  • In: Acta Dermato-Venereologica. - : Medical Journals Sweden AB. - 0001-5555 .- 1651-2057. ; 82:5, s. 341-346
  • Journal article (peer-reviewed)abstract
    • Ninety-five percent of patients with palmoplantar pustulosis are smokers at onset of the disease. The aim of this study was to determine whether these patients have serum antibodies to nicotinic acetylcholine receptors (nAChR ab) and if their sera induce a specific immunofluorescence in normal palmar skin. Sera from 45 patients with palmoplantar pustulosis and 23 patients with chronic hand eczema were analysed for muscle nAChR ab, and immunofluorescence was performed on healthy palmar skin. Forty-two percent of the patients with palmoplantar pustulosis but none of the eczema patients had raised levels of nAChR ab. Immunofluorescence showed staining on endothelial cells in the papillary dermis in 47% of all sera from patients with palmoplantar pustulosis and in those with nAChR ab in 68%. On palmar skin from smokers there was also a staining of the sweat duct. Sera from patients with chronic hand eczema were negative. Our findings indicate that palmoplantar pustulosis is an autoimmune disease, possibly induced by smoking.
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2.
  • Mustafa, Awder (author)
  • Circulating immune complexes in atherosclerotic vascular disease
  • 2001
  • Doctoral thesis (other academic/artistic)abstract
    • We have investigated the association of the humoral immune factors circulating immune complexes (CICs) and autoantibodies against cardiolipin (aCL) and oxidatively modified LDL (oxLDL) to atherosclerotic vascular diseases. In a prospective nested case-control study, in which healthy 50-year-old men were followed for 20 years, the prevalence of elevated CICs and the concentration of CICs were higher in men who developed myocardial infarction. (MI) than in those who remained healthy. CICs was a strong and independent risk factor. There was a positive relation between the levels of CICs and IgG-aCL in men who developed Nil. The level of IgG-aCL and the prevalence of elevated IgG- and IgM-aCL were higher in those who developed MI and had CICs than in those without CICs. Among men homozygous for C4 null alleles, those who developed MI had higher concentrations of CICs than did those who remained healthy. In a five-year prospective study, CICs and antibodies against oxLDL were associated with progression of coronary atherosclerosis in young dyshpoproteinemic men suffering from coronary artery disease. In 18% of patients who had survived a premature MI, CICs were present in high concentrations many years after the event. Antibodies of the IgG isotype predominated in CICs. Half of the patients with persistent high CICs had alimentary proteins in the immune complexes. A rise in CICs, signs of activation of the complement cascade, and a rise in plasma concentrations of vonWillebrand factor antigen were evident within one week in four young patients subjected to a 2-week elimination diet followed by challenge with the alimentary antigen in question. Elevated levels of CICs were present in patients with premature peripheral atherosclerosis and null alleles of C4A (C4A*QO) enhanced the propensity to ICs formation. CICs were increased in patients with diabetes, and especially in those with vascular complications. The concentrations of aCL were relatively higher in CICs than in serum. The concentration and prevalence of CICs were increased in patients with C4A*QO. Patients with vascular complications had more often C4A*QO than C4B*QO.
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